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Items: 1 to 50 of 57

1.

Identification of a Mutation in SPG11 in an Iranian Patient with Spastic Paraplegia and Ears of the Lynx Sign.

Sayad A, Akbari MT, Hesami O, Ghafouri-Fard S, Taheri M.

J Mol Neurosci. 2020 Feb 10. doi: 10.1007/s12031-020-01501-2. [Epub ahead of print]

PMID:
32040826
2.

Association between HLA alleles and risk of celiac disease in Iranian patients.

Fallah H, Akbari MT, Mirzajani S, Ranjbaran F, Mehdizadeh B, Sayad A, Taheri M.

Hum Antibodies. 2019 Oct 18. doi: 10.3233/HAB-190398. [Epub ahead of print]

PMID:
31658053
3.

Observation of nine previously reported and 10 non-reported SLC4A11 mutations among 20 Iranian CHED probands and identification of an MPDZ mutation as possible cause of CHED and FECD in one family.

Moazzeni H, Javadi MA, Asgari D, Khani M, Emami M, Moghadam A, Panahi-Bazaz MR, Hosseini Tehrani M, Karimian F, Hosseini B, Nekuie Moghadam T, Hassanpour H, Akbari MT, Elahi E.

Br J Ophthalmol. 2019 Aug 16. pii: e314377. doi: 10.1136/bjophthalmol-2019-314377. [Epub ahead of print]

PMID:
31420327
4.

Association between human leucocyte antigen alleles and risk of stroke in Iranian population.

Sayad A, Akbari MT, Inoko H, Khazaei M, Mehdizadeh B, Taheri M, Ghafouri-Fard S.

Int J Immunogenet. 2019 Jun;46(3):179-191. doi: 10.1111/iji.12421. Epub 2019 Mar 18.

PMID:
30884125
5.

Association of HLA alleles with autism.

Sayad A, Akbari MT, Noroozi R, Omrani MD, Inoko H, Taheri M, Ghafouri-Fard S.

Neuropsychiatr Dis Treat. 2018 Nov 27;14:3259-3265. doi: 10.2147/NDT.S186673. eCollection 2018.

6.

Transcriptome mining of non-BRCA1/A2 and BRCA1/A2 familial breast cancer.

Akbari V, Kallhor M, Akbari MT.

J Cell Biochem. 2019 Jan;120(1):575-583. doi: 10.1002/jcb.27413. Epub 2018 Aug 20.

PMID:
30125992
7.

Assessing the Diagnostic Value of Plasma-Free DNA in Prostate Cancer Screening

Seyedolmohadessin SM, Akbari MT, Nourmohammadi Z, Basiri A, Pourmand G.

Iran Biomed J. 2018 Sep;22(5):331-7. Epub 2018 Feb 24.

8.

Identification and characterization of a novel recessive KCNQ1 mutation associated with Romano-Ward Long-QT syndrome in two Iranian families.

Zafari Z, Dalili M, Zeinali S, Saber S, Fazeli Far AF, Akbari MT.

J Electrocardiol. 2017 Nov - Dec;50(6):912-918. doi: 10.1016/j.jelectrocard.2017.07.012. Epub 2017 Jul 12.

PMID:
29033053
9.

In Vitro Hb Production in B-thalassemia Patients Is Not a Predictor of Clinical Responsiveness to Hydroxyurea.

Mahdavi MR, Pourfarzad F, Kosaryan M, Akbari MT.

Iran J Public Health. 2017 Jul;46(7):948-956.

10.

Association study of the common polymorphisms in the folate-methionine pathway with retinoblastoma.

Soleimani E, Saliminejad K, Akbari MT, Kamali K, Ahani A.

Ophthalmic Genet. 2016 Dec;37(4):384-387. Epub 2016 Feb 25.

PMID:
26914443
11.

Expression of CXCL6 and BBS5 that may be glaucoma relevant genes is regulated by PITX2.

Moazzeni H, Akbari MT, Yazdani S, Elahi E.

Gene. 2016 Nov 15;593(1):76-83. doi: 10.1016/j.gene.2016.08.019. Epub 2016 Aug 9.

PMID:
27520585
12.

Evaluation of point mutations in dystrophin gene in Iranian Duchenne and Becker muscular dystrophy patients: introducing three novel variants.

Haghshenas M, Akbari MT, Karizi SZ, Deilamani FK, Nafissi S, Salehi Z.

J Genet. 2016 Jun;95(2):325-9.

13.

Whole Exome Sequencing of Chronic Myeloid Leukemia Patients.

Sabri S, Keyhani M, Akbari MT.

Iran J Public Health. 2016 Mar;45(3):346-52.

14.

HLA genes as modifiers of response to IFN-β-1a therapy in relapsing-remitting multiple sclerosis.

Mazdeh M, Taheri M, Sayad A, Bahram S, Omrani MD, Movafagh A, Inoko H, Akbari MT, Noroozi R, Hajilooi M, Solgi G.

Pharmacogenomics. 2016 Apr;17(5):489-98. doi: 10.2217/pgs.16.2. Epub 2016 Mar 29.

PMID:
27020477
15.

Population data of 13 nonCODIS STR markers located inside the 6 nonsyndromic oculocutaneous albinism genes.

Khordadpoor Deilamani F, Akbari MT.

Int J Legal Med. 2016 Nov;130(6):1485-1486. Epub 2016 Mar 1.

PMID:
26932870
16.

Homozygosity mapping in albinism patients using a novel panel of 13 STR markers inside the nonsyndromic OCA genes: introducing 5 novel mutations.

Khordadpoor-Deilamani F, Akbari MT, Karimipoor M, Javadi GR.

J Hum Genet. 2016 May;61(5):373-9. doi: 10.1038/jhg.2015.167. Epub 2016 Jan 28.

PMID:
26818737
17.
18.

Methionine synthase A2756G variation is associated with the risk of retinoblastoma in Iranian children.

Akbari MT, Naderi A, Saremi L, Sayad A, Irani S, Ahani A.

Cancer Epidemiol. 2015 Dec;39(6):1023-5. doi: 10.1016/j.canep.2015.11.002. Epub 2015 Nov 18.

PMID:
26595280
20.

Double Heterozygosity of BRCA2 and STK11 in Familial Breast Cancer Detected by Exome Sequencing.

Ataei-Kachouei M, Nadaf J, Akbari MT, Atri M, Majewski J, Riazalhosseini Y, Garshasbi M.

Iran J Public Health. 2015 Oct;44(10):1348-52.

21.

Sequence analysis of tyrosinase gene in ocular and oculocutaneous albinism patients: introducing three novel mutations.

Khordadpoor-Deilamani F, Akbari MT, Karimipoor M, Javadi G.

Mol Vis. 2015 Jul 10;21:730-5. eCollection 2015.

22.

HLA-A*26 and susceptility of iranian patients with non-Hodgkin lymphoma.

Sayad A, Akbari MT, Mehdizadeh M, Taheri M, Hajifathali A.

Iran J Immunol. 2014 Dec;11(4):269-74. doi: IJIv11i4A5.

23.

The Association of HLA Class 1 and Class 2 Antigens with Multiple Myeloma in Iranian Patients.

Sayad A, Akbari MT, Mehdizadeh M, Roshandel E, Abedinpour S, Hajifathali A.

Turk J Haematol. 2014 Dec 5;31(4):388-93. doi: 10.4274/tjh.2013.0098.

24.

The association of HLA-class I and class II with Hodgkin's lymphoma in Iranian patients.

Sayad A, Akbari MT, Mehdizadeh M, Movafagh A, Hajifathali A.

Biomed Res Int. 2014;2014:231236. doi: 10.1155/2014/231236. Epub 2014 May 21.

25.

Thiamine-responsive megaloblastic anemia syndrome with Ebstein anomaly: a case report.

Akbari MT, Zare Karizi S, Mirfakhraie R, Keikhaei B.

Eur J Pediatr. 2014 Dec;173(12):1663-5. doi: 10.1007/s00431-013-2237-7. Epub 2013 Dec 20.

PMID:
24357267
26.

Rapid detection of RB1 recurrent mutations in retinoblastoma by ARMS-PCR.

Saliminejad K, Behnam B, Akbari MT, Khorshid HR, Ghassemi F, Amoli FA, Akhondi MM, Vosoogh P, Naseripour M, Ahani A.

J Genet. 2013 May 29;92(2):e36-40. No abstract available.

27.

The association of -475 and -631 interleukin-2 gene polymorphism with multiple sclerosis in Iranian patients.

Sayad A, Allameh A, Sayad A, Noruzinia M, Akbari MT, Sarzaeem A, Akbar A, Haji Hoseini R.

Cell J. 2013 Summer;15(2):124-9. Epub 2013 Jul 2.

28.

Investigation The Role of Gender on The HLA-DRB1 and -DQB1 Association with Type 1 Diabetes Mellitus in Iranian Patients.

Sayad A, Akbari MT, Pajouhi M, Mostafavi F, Kazemnejad A, Zamani M.

Cell J. 2013 Summer;15(2):108-15. Epub 2013 Jul 2.

29.

Detection of Rare Beta Globin Gene Mutation [+22 5UTR(G>A)] in an Infant, Despite Prenatal Screening.

Mahdavi MR, Karami H, Akbari MT, Jalali H, Roshan P.

Case Rep Hematol. 2013;2013:906292. doi: 10.1155/2013/906292. Epub 2013 Apr 14.

30.

Evaluation and comparison of soluble transferrin receptor in thalassemia carriers and iron deficient patients.

Khatami S, Dehnabeh SR, Mostafavi E, Kamalzadeh N, Yaghmaei P, Saeedi P, Shariat F, Bagheriyan H, Zeinali S, Akbari MT.

Hemoglobin. 2013;37(4):387-95. doi: 10.3109/03630269.2013.780248. Epub 2013 Apr 12.

PMID:
23581600
31.

Promoter hypermethylation of estrogen receptor alpha gene is correlated to estrogen receptor negativity in Iranian patients with sporadic breast cancer.

Izadi P, Noruzinia M, Karimipoor M, Karbassian MH, Akbari MT.

Cell J. 2012 Summer;14(2):102-9. Epub 2012 Aug 31.

32.

Screening for large rearrangements of the RB1 gene in Iranian patients with retinoblastoma using multiplex ligation-dependent probe amplification.

Ahani A, Akbari MT, Saliminejad K, Behnam B, Akhondi MM, Vosoogh P, Ghassemi F, Naseripour M, Bahoush G, Khorshid HR.

Mol Vis. 2013;19:454-62. Epub 2013 Feb 22.

33.

Positive association of Apolipoprotein E4 polymorphism with recurrent pregnancy loss in Iranian patients.

Asgari N, Akbari MT, Zare S, Babamohammadi G.

J Assist Reprod Genet. 2013 Feb;30(2):265-8. doi: 10.1007/s10815-012-9897-5. Epub 2013 Jan 8.

34.

A girl with 45,X/46,XX Turner syndrome and salt wasting form of congenital adrenal hyperplasia due to regulatory changes.

Rabbani B, Mahdieh N, Sayarifar F, Ashtiani MT, New M, Parsa A, Akbari MT, Rabbani A.

Clin Lab. 2012;58(9-10):1063-6.

PMID:
23163125
35.

Identification of α-globin chain variants: a report from Iran.

Akbari MT, Hamid M.

Arch Iran Med. 2012 Sep;15(9):564-7. doi: 012159/AIM.0011.

36.

Screening of OTOF mutations in Iran: a novel mutation and review.

Mahdieh N, Shirkavand A, Rabbani B, Tekin M, Akbari B, Akbari MT, Zeinali S.

Int J Pediatr Otorhinolaryngol. 2012 Nov;76(11):1610-5. doi: 10.1016/j.ijporl.2012.07.030. Epub 2012 Aug 18.

PMID:
22906306
37.

Detection of deletions/duplications in α-globin gene cluster by multiplex ligation-dependent probe amplification.

Nezhat N, Akbari MT.

Genet Test Mol Biomarkers. 2012 Jul;16(7):684-8. doi: 10.1089/gtmb.2011.0251. Epub 2012 Jun 25.

PMID:
22731639
38.

Clinical features, DYT1 mutation screening and genotype-phenotype correlation in patients with dystonia from Iran.

Akbari MT, Zand Z, Shahidi GA, Hamid M.

Med Princ Pract. 2012;21(5):462-6. doi: 10.1159/000336783. Epub 2012 Apr 6.

39.

Large-scale screening of mitochondrial DNA mutations among Iranian patients with prelingual nonsyndromic hearing impairment.

Montazer Zohour M, Tabatabaiefar MA, Dehkordi FA, Farrokhi E, Akbari MT, Chaleshtori MH.

Genet Test Mol Biomarkers. 2012 Apr;16(4):271-8. doi: 10.1089/gtmb.2011.0176. Epub 2011 Nov 11.

PMID:
22077646
40.

Mutation analysis of the CYP21A2 gene in the Iranian population.

Rabbani B, Mahdieh N, Ashtiani MT, Larijani B, Akbari MT, New M, Parsa A, Schouten JP, Rabbani A.

Genet Test Mol Biomarkers. 2012 Feb;16(2):82-90. doi: 10.1089/gtmb.2011.0099. Epub 2011 Oct 21.

41.

Dystrophin gene mutation analysis in Iranian males and females using multiplex polymerase chain reaction and multiplex ligation-dependent probe amplification methods.

Khordadpoor-Deilamani F, Akbari MT, Nafissi S, Zamani G.

Genet Test Mol Biomarkers. 2011 Dec;15(12):893-9. doi: 10.1089/gtmb.2011.0057. Epub 2011 Aug 4.

PMID:
21815800
42.

RB1 gene mutations in Iranian patients with retinoblastoma: report of four novel mutations.

Ahani A, Behnam B, Khorshid HR, Akbari MT.

Cancer Genet. 2011 Jun;204(6):316-22. doi: 10.1016/j.cancergen.2011.04.007.

PMID:
21763628
43.
44.

Transient expression assay of Agamma-588 (A/G) mutations in the K562 cell line.

Hamid M, Mahjoubi F, Akbari MT, Khanahmad H, Jamshidi F, Zeinali S, Karimipoor M.

Iran Biomed J. 2011;15(1-2):15-21.

45.

Determination of exon 7 SMN1 deletion in Iranian patients and heterozygous carriers by quantitative real-time PCR.

Akbari MT, Noruzinia M, Mozdarani H, Hamid M.

J Genet. 2011 Apr;90(1):133-6. No abstract available.

46.

Molecular Diagnosis of Congenital Adrenal Hyperplasia in Iran: Focusing on CYP21A2 Gene.

Rabbani B, Mahdieh N, Haghi Ashtiani MT, Akbari MT, Rabbani A.

Iran J Pediatr. 2011 Jun;21(2):139-50.

47.

The Frequency of DYT1 (GAG Deletion) Mutation in Primary Dystonia Patients from Iran.

Hamid M, Akbari MT, Shahidi GA, Zand Z.

Cell J. 2011 Spring;13(1):55-8. Epub 2011 Apr 21.

48.

Impact of consanguineous marriages in GJB2-related hearing loss in the Iranian population: a report of a novel variant.

Mahdieh N, Rabbani B, Shirkavand A, Bagherian H, Movahed ZS, Fouladi P, Rahiminejad F, Masoudifard M, Akbari MT, Zeinali S.

Genet Test Mol Biomarkers. 2011 Jul-Aug;15(7-8):489-93. doi: 10.1089/gtmb.2010.0145. Epub 2011 Mar 9.

PMID:
21388256
49.

Investigation of GJB6 large deletions in Iranian patients using quantitative real-time PCR.

Mahdieh N, Raeisi M, Shirkavand A, Bagherian H, Akbari MT, Zeinali S.

Clin Lab. 2010;56(9-10):467-71.

PMID:
21086793
50.

Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: implication for genetic counseling.

Mahdieh N, Shirkavand A, Raeisi M, Akbari MT, Tekin M, Zeinali S.

Biochem Biophys Res Commun. 2010 Nov 12;402(2):305-7. doi: 10.1016/j.bbrc.2010.10.021. Epub 2010 Oct 19.

PMID:
20937258

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